Taiwan FDA registration 67f5998385d4e52d24ded91156a40c2b
"ACRO" Adenovirus test kit (Non-Sterile)
TW: "愛可羅" 腺病毒檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Jun 26, 2018 – Jun 26, 2028ActiveRegistration details
- Analysis ID
- 67f5998385d4e52d24ded91156a40c2b
- License Form
- Ministry of Health Medical Device Import No. 019236
- Customs Code
- DHA09401923601
Company information
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 26, 2018
- Expiry Date
- Jun 26, 2028
About this record
Access comprehensive regulatory information for "ACRO" Adenovirus test kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 67f5998385d4e52d24ded91156a40c2b and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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